TY  - GEN
AU  - Lalani,S R
AU  - Thakuria,J V
AU  - Cox,G F
AU  - Wang,X
AU  - Bi,W
AU  - Bray,M S
AU  - Shaw,C
AU  - Cheung,S W
AU  - Chinault,A C
AU  - Boggs,B A
AU  - Ou,Z
AU  - Brundage,E K
AU  - Lupski,J R
AU  - Gentile,J
AU  - Waisbren,S
AU  - Pursley,A
AU  - Ma,L
AU  - Khajavi,M
AU  - Zapata,G
AU  - Friedman,R
AU  - Kim,J J
AU  - Towbin,J A
AU  - Stankiewicz,P
AU  - Schnittger,S
AU  - Hansmann,I
AU  - Ai,T
AU  - Sood,S
AU  - Wehrens,X H
AU  - Martin,J F
AU  - Belmont,J W
AU  - Potocki,L
TI  - 20p12.3 microdeletion predisposes to Wolff-Parkinson-White syndrome with variable neurocognitive deficits
SN  - 1468-6244
PY  - 2009///0521
KW  - Adult
KW  - Alagille Syndrome
KW  - genetics
KW  - Animals
KW  - Bone Morphogenetic Protein 2
KW  - Calcium-Binding Proteins
KW  - Cognition Disorders
KW  - Comparative Genomic Hybridization
KW  - Electrocardiography
KW  - Facies
KW  - Female
KW  - Gene Dosage
KW  - Humans
KW  - Infant
KW  - Intercellular Signaling Peptides and Proteins
KW  - Jagged-1 Protein
KW  - Male
KW  - Membrane Proteins
KW  - Mice
KW  - Mice, Transgenic
KW  - Oligonucleotide Array Sequence Analysis
KW  - Sequence Deletion
KW  - Serrate-Jagged Proteins
KW  - Wolff-Parkinson-White Syndrome
N1  - Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1136/jmg.2008.061002
ER  -